Zenthera: A High-Speed Antimicrobial Resistance Prediction Pipeline Using K-Mer Analysis and Tree-Based Ensembles
Authors
Dept. of Computer Engineering Fr. Conceicao Rodrigues College of Engineering Bandra-Mumbai, India (India)
Dept. of Computer Engineering Fr. Conceicao Rodrigues College of Engineering Bandra-Mumbai, India (India)
Dept. of Computer Engineering Fr. Conceicao Rodrigues College of Engineering Bandra-Mumbai, India (India)
Dept. of Computer Engineering Fr. Conceicao Rodrigues College of Engineering Bandra-Mumbai, India (India)
Dept. of Computer Engineering Fr. Conceicao Rodrigues College of Engineering Bandra-Mumbai, India (India)
Article Information
DOI: 10.51584/IJRIAS.2026.11050066
Subject Category: Bioinformatics and Applied Machine Learning
Volume/Issue: 11/5 | Page No: 786-796
Publication Timeline
Submitted: 2026-04-30
Accepted: 2026-05-05
Published: 2026-05-30
Abstract
Antimicrobial resistance (AMR) is a rapidly growing problem in modern medicine. When doctors don’t know exactly which bacteria is causing an infection, they often prescribe broad-spectrum antibiotics. This practice actually speeds up the evolution of drug-resistant pathogens. The standard way to figure out which drug works is Antibiotic Susceptibility Testing (AST). However, AST requires physically growing bacteria in a lab, which can take anywhere from 24 to 72 hours. In this paper, we introduce Zenthera, a computational biology pipeline designed to skip this culturing step entirely. We built a system that uses raw Whole Genome Sequencing (WGS) data to predict resistance against 14 different antibiotics in real-time. Instead of slow genetic alignment, our pipeline uses a k-mer (k=7) frequency approach combined with TF-IDF vectorization. We trained Random Forest and XGBoost models on a dataset of over 100,000 bacterial genomes, achieving an average accuracy of 92.4% and an F1-score of 0.91. Because we used GPU acceleration, our system can process a genome and provide a clinical prediction in less than a second. To make this actually usable for doctors, we deployed the models inside a full-stack web application. Zenthera shows that we can eliminate the waiting time of traditional lab tests without losing accuracy.
Keywords
Antimicrobial Resistance, Machine Learning, K-mers, Whole Genome Sequencing, Tree-Based Ensembles
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References
1. J. O’Neill, Tackling Drug-Resistant Infections Globally: Final Report and Recommendations. Review on Antimicrobial Resistance, 2016.Available: https://amr-review.org/Publications.html [Google Scholar] [Crossref]
2. A. Kumar et al., “Initiation of inappropriate antimicrobial therapy results in a fivefold reduction of survival in human septic shock,” Chest, vol. 130, no. 4, pp. 929-939, 2006. DOI: https://doi.org/10.1378/chest.130.4.929 [Google Scholar] [Crossref]
3. J. I. Kim et al., “Machine Learning for Antimicrobial Resistance Prediction,” Clinical Microbiology Reviews, vol. 35, 2022. DOI: https://doi.org/10.1128/cmr.00224-21 [Google Scholar] [Crossref]
4. J. J. Davis et al., “The PATRIC Bioinformatics Resource Center,” Nucleic Acids Research, vol. 48, 2020. DOI: https://doi.org/10.1093/nar/ gkz943 [Google Scholar] [Crossref]
5. B. P. Alcock et al., “CARD 2020,” Nucleic Acids Research, vol. 48, 2020. DOI: https://doi.org/10.1093/nar/gkz935 [Google Scholar] [Crossref]
6. M. Nguyen et al., “Using machine learning to predict antimicrobial MICs,” Journal of Clinical Microbiology, vol. 57, 2020. DOI: https://doi.org/10.1128/JCM.01260-20 [Google Scholar] [Crossref]
7. L. Breiman, “Random Forests,” Machine Learning, vol. 45, 2001. DOI: https://doi.org/10.1023/A:1010933404324 [Google Scholar] [Crossref]
8. T. Chen and C. Guestrin, “XGBoost: A Scalable Tree Boosting System,” in Proceedings of KDD, 2016. DOI: https://doi.org/10.1145/2939672. 2939785 [Google Scholar] [Crossref]
9. B. Y. Lee et al., “The economic burden of antimicrobial resistance in the United States,” Infection Control & Hospital Epidemiology, vol. 42, no. 1, 2021. DOI: https://doi.org/10.1017/ice.2020.1264 [Google Scholar] [Crossref]
10. L. B. Rice, “Federal funding for the study of antimicrobial resistance in nosocomial pathogens: no ESKAPE,” The Journal of Infectious Diseases, vol. 197, no. 8, pp. 1079-1081, 2008. DOI: https://doi.org/ 10.1086/533452 [Google Scholar] [Crossref]
11. G. Salton and C. Buckley, “Term-weighting approaches in automatic text retrieval,” Information Processing & Management, vol. 24, no. 5,pp. 513-523, 1988. DOI: https://doi.org/10.1016/0306-4573(88)90021-0 [Google Scholar] [Crossref]
12. A. Esteva et al., “A guide to deep learning in healthcare,” Nature Medicine, vol. 25, no. 1, pp. 24-29, 2019. DOI: https://doi.org/10.1038/s41591-018-0316-z [Google Scholar] [Crossref]
13. T. Ching et al., “Opportunities and obstacles for deep learning in biology and medicine,” Journal of The Royal Society Interface, vol. 15, 2018.DOI: https://doi.org/10.1098/rsif.2017.0387 [Google Scholar] [Crossref]
14. N. Rieke et al., “The future of digital health with Federated Learning,” NPJ Digital Medicine, vol. 3, no. 1, pp. 1-7, 2020. DOI: https://doi.org/10.1038/s41746-020-00323-1 [Google Scholar] [Crossref]
15. J. Quick et al., “Real-time, portable genome sequencing for Ebola surveillance,” Nature, vol. 530, no. 7589, pp. 228-232, 2016. DOI: https://doi.org/10.1038/nature16996 [Google Scholar] [Crossref]